Effectiveness of Four Transition Dietary Regimens in the Hospital Management of Children With Kwashiorkor.

NCT ID: NCT05015257

Last Updated: 2023-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-15

Study Completion Date

2023-08-31

Brief Summary

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In Burkina Faso the number of severely acute malnourished (SAM) children successfully treated has increased since the implementation of community-based management of acute malnutrition. SAM children with oedema have a higher risk of dying than SAM without oedema; they require inpatient care. Several theories have been proposed to explain the pathophysiology of oedema in SAM, but its etiology remains unclear. Knowledge on the nutritional adequacy of therapeutic regimens in kwashiorkor is limited. The World Health Organization (WHO) recommends to use in the treatment of complicated SAM a therapeutic milk 'F75' in the stabilization phase; F75+ready-to-use therapeutic foods (RUTF) or F100 at the transition phase. Alternatively the local formulas (maize flour, milk powder, oil, sugar, mineral-vitamin complex CMV) can be used in case of shortage or intolerance.

At the Nutritional Rehabilitation and Education Center of the University Hospital of Bobo Dioulasso it was found that some SAM children whose oedema resolved under F75 in the stabilization phase, re-developed oedema as they entered the transition phase with RUTF. RUTF has the same nutritional value as F100 but contains iron unlike F100 (\<0.07 mg/100 mL). It was observed that RUTF in some cases may be associated with higher mortality, probably due to high iron content (10-14 mg/100 g), which may increase the risk of infections and the formation of free radicals, thereby increasing damage to the body's cells. Clinical trials evaluating the current guidelines for the treatment of SAM with oedema are scarce. A better understanding of the risk factors affecting the effectiveness of the nutritional therapeutic protocol for children with Kwashiorkor will be useful to improve their care.

The main objective of this study is to determine whether the use of transition phase diets (Plumpy-Nut®+F75 or F100 or alternative F75+/- CMV+ Plumpy-Nut®) affect oedema resolving in Kwashiorkor children and to investigate the underlying factors for the relapse or non-responsiveness to the therapeutic treatment.

Detailed Description

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Severe acute malnutrition (SAM) is a life threatening condition that requires urgent attention and appropriate management to reduce mortality and promote recovery among children. SAM is defined by 1) a weight-for-height Z-score more than three standard deviations (SD) below the median based on the 2006 WHO growth standards, 2) a mid-upper arm circumference (MUAC) of less than 115 mm or 3) by the presence of nutritional edema. Signs such as edema, mucocutaneous changes, hepatomegaly, lethargy, anorexia, anemia, severe immune deficiency and rapid progression to mortality characterize a state commonly coined as "complicated SAM". Kwashiorkor (SAM with edema) is one of the forms of complicated SAM commonly distinguished by the unmistakable presence of bipedal edema. Kwashiorkor is characterized by the following clinical signs: 1) edemas symmetrical, painless, soft, bilateral, ascending, pitting; 2) lesions of the skin and integuments; 3) ulcerations and depigmentation; 4) alopecia; 5) constant weight loss marked by edema; 6) hepatomegaly; 7) clinical anemia; 8) intestinal transit disorders: persistent diarrhea, vomiting; 9) anorexia and behavioral disorders (apathy).

Severe acute malnutrition results in high mortality rates of up to half a million child deaths annually. Undernourished children are at higher risk of mortality ranging from three-times more risk among children with moderate malnutrition to 10-times in SAM children compared to well-nourished children.

The objective of this study is to determine whether the use of different transition phase diets affect oedema resolving in Kwashiorkor children and to investigate the underlying factors for the relapse or non-responsiveness to the therapeutic treatment.

Hypotheses to be tested

* The first hypothesis is that RUTF (Plumpy-Nut®) because of its content in iron may compromise the effectiveness of the transition phase in children with kwashiorkor
* The second hypothesis is that underlying factors including co-morbidities and epigenetics may explain a difference in response to therapeutic regimens

This is an open label randomized controlled trial to test the effectiveness of four used transition phase diets in Kwashiorkor children in their transition to the rehabilitation phase. The four dietary regimens that will be tested are:

1. F100;
2. RUTF+F75;
3. RUTF+alternative F75 with complex mineral-vitamin (CMV); and
4. RUTF+alternative F75 without CMV.

When it is decided to move to the transition phase, the child will be assigned to one of the treatments depending on the treatment received during the stabilization phase and the results of the appetite test. That is a child who accepts the Plumpy Nut will receive it in combination with their regimen they had during the stabilization phase. If a child does not accept Plumpy Nut, then they will received F100 regardless of their initial therapeutic food regimen.

* For those who received F75 in the stabilization phase, they will receive standard F75 + Plumpy Nut
* For those who received alternative F75 with CMV in the stabilization phase, they will receive alternative F75 with CMV + Plumpy Nut®
* For those who received alternative F75 without CMV in the stabilization phase, they will receive alternative F75 without CMV + Plumpy Nut®.

Conditions

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Severe Acute Malnutrition Kwashiorkor Nutritional Edema

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

This is an open label randomized controlled trial to test the effectiveness of four diets in Kwashiorkor children in their transition phase.

When it is decided to move to the transition phase, the child will be assigned to one of the treatments depending on the treatment received during the stabilization phase and the results of the appetite test. That is a child who accepts the Plumpy Nut will receive it in combination with their regimen they had during the stabilization phase. If a child does not accept Plumpy Nut, then they will received F100 regardless of their initial therapeutic food regimen.

* For those who received F75 in the stabilization phase, they will receive standard F75 + Plumpy Nut
* For those who received alternative F75 with CMV in the stabilization phase, they will receive alternative F75 with CMV + Plumpy Nut®
* For those who received alternative F75 without CMV in the stabilization phase, they will receive alternative F75 without CMV + Plumpy Nut®.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Standard F100

If the test of appetite at the end of the stabilization phase is negative (the child does not accept the Plumpynut)

Group Type ACTIVE_COMPARATOR

Standard F100

Intervention Type DIETARY_SUPPLEMENT

100 kcal and 3 g protein per 100 ml

Standard F75+Plumpynut

If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Standard F75 during the stabilization phase

Group Type EXPERIMENTAL

Standard F75 + Plumpynut

Intervention Type DIETARY_SUPPLEMENT

Standard F75 with ready to-use therapeutic food (Plumpynut)

Alternative F75 with CMV +Plumpynut

If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Alternative F75 with CMV during the stabilization phase

Group Type EXPERIMENTAL

Alternative F75 with CMV + Plumpynut

Intervention Type DIETARY_SUPPLEMENT

Alternative F75 containing CMV with ready to-use therapeutic food (Plumpynut)

Alternative F75 without CMV +Plumpynut

If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Alternative F75 without CMV during the stabilization phase

Group Type EXPERIMENTAL

Alternative F75 without CMV + Plumpynut

Intervention Type DIETARY_SUPPLEMENT

Alternative F75 with no CMV with ready to-use therapeutic food (Plumpynut)

Interventions

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Standard F100

100 kcal and 3 g protein per 100 ml

Intervention Type DIETARY_SUPPLEMENT

Standard F75 + Plumpynut

Standard F75 with ready to-use therapeutic food (Plumpynut)

Intervention Type DIETARY_SUPPLEMENT

Alternative F75 with CMV + Plumpynut

Alternative F75 containing CMV with ready to-use therapeutic food (Plumpynut)

Intervention Type DIETARY_SUPPLEMENT

Alternative F75 without CMV + Plumpynut

Alternative F75 with no CMV with ready to-use therapeutic food (Plumpynut)

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Severe acute malnutrition defined as the presence of edema
* Who are admitted and treated in the refeeding center (CREN) of the CHUSS
* Aged between 6 and 59 Months
* Parental Signed informed consent form
* Recruited in the first phase of the treatment and successfully admitted to the transition phase

Exclusion Criteria

* SAM without edema
* Moderate acute malnutrition (MAM)
* Did not improve during the stabilization phase
Minimum Eligible Age

6 Months

Maximum Eligible Age

59 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Institut de Recherche en Sciences de la Sante, Burkina Faso

OTHER_GOV

Sponsor Role collaborator

University Hospital Sourô Sanou of Bobo Dioulasso (Burkina Faso)

UNKNOWN

Sponsor Role collaborator

Centre Muraz

OTHER

Sponsor Role collaborator

University Ghent

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stefaan De Henauw, Md. PhD

Role: PRINCIPAL_INVESTIGATOR

University Ghent

Souheila Abbeddou, MSc. PhD

Role: PRINCIPAL_INVESTIGATOR

University Ghent

Jerome Some, Md. PhD

Role: PRINCIPAL_INVESTIGATOR

Institut de Recherche en Sciences de la Sante, Burkina Faso

Bintou Sanogo, MSc. Md.

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire Souro, Bobo Dioulasso, Burkina Faso.

Locations

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Centre Hospitalier Universitaire Souro

Bobo-Dioulasso, Bobo Dioulasso, Burkina Faso

Site Status

Countries

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Burkina Faso

References

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Gopalan C. Kwashiorkor and marasmus: evolution and distinguishing features. 1968. Natl Med J India. 1992 May-Jun;5(3):145-51. No abstract available.

Reference Type BACKGROUND
PMID: 1306670 (View on PubMed)

Nguefack F, Adjahoung CA, Keugoung B, Kamgaing N, Dongmo R. [Hospital management of severe acute malnutrition in children with F-75 and F-100 alternative local preparations: results and challenges]. Pan Afr Med J. 2015 Aug 31;21:329. doi: 10.11604/pamj.2015.21.329.6632. eCollection 2015. French.

Reference Type BACKGROUND
PMID: 26587175 (View on PubMed)

Singh K, Badgaiyan N, Ranjan A, Dixit HO, Kaushik A, Kushwaha KP, Aguayo VM. Management of children with severe acute malnutrition: experience of Nutrition Rehabilitation Centers in Uttar Pradesh, India. Indian Pediatr. 2014 Jan;51(1):21-5. doi: 10.1007/s13312-014-0328-9. Epub 2013 Jul 5.

Reference Type BACKGROUND
PMID: 24277964 (View on PubMed)

Smith MI, Yatsunenko T, Manary MJ, Trehan I, Mkakosya R, Cheng J, Kau AL, Rich SS, Concannon P, Mychaleckyj JC, Liu J, Houpt E, Li JV, Holmes E, Nicholson J, Knights D, Ursell LK, Knight R, Gordon JI. Gut microbiomes of Malawian twin pairs discordant for kwashiorkor. Science. 2013 Feb 1;339(6119):548-54. doi: 10.1126/science.1229000. Epub 2013 Jan 30.

Reference Type BACKGROUND
PMID: 23363771 (View on PubMed)

Related Links

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https://www.who.int/publications/i/item/9789241506328

World Health Organization (2013) WHO guideline: updates on the management of severe acute malnutrition in infants and children

https://www.unicef.fr/article/malnutrition-la-situation-au-burkina-faso

Enquête Nutritionnelle Nationale SMART 2016 au Burkina Faso. 2016 ; 47p

https://www.humanitarianresponse.info/sites/www.humanitarianresponse.info/files/documents/files/protocole_pcima_bf_janv_2015.pdf

Ministère de la Sante au Burkina Faso. Protocol National : Prise en charge intégrée de la malnutrition aigüe (PCIMA). 2014

Other Identifiers

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BC-09443-B

Identifier Type: -

Identifier Source: org_study_id

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